Amidine
Amidines are organic compounds with the functional group RCNR2, where the R groups can be the same or different. They are the imine derivatives of amides. The simplest amidine is formamidine, HCNH2.
Examples of amidines include:
- DBU
- diminazene
- benzamidine
- Pentamidine
- Paranyline
Preparation
A common route to primary amidines is the Pinner reaction. Reaction of the nitrile with alcohol in the presence of acid gives an iminoether. Treatment of the resulting compound with ammonia then completes the conversion to the amidine. Instead of using a Bronsted acid, Lewis acids such as aluminium trichloride promote the direct amination of nitriles, or, in certain exceptional cases, of amides. Dimethylformamide acetal reacts with primary amines to give amidines:Catalysis is likewise not required for direct amination of an imidoyl chloride.
Amidines are also prepared by the addition of organolithium reagents to diimines, followed by protonation or alkylation.
Acid-base chemistry
Amidines are much more basic than amides and are among the strongest uncharged/unionized bases.Protonation occurs at the sp2-hybridized nitrogen. This occurs because the positive charge can be delocalized onto both nitrogen atoms. The resulting cationic species is known as an amidinium ion and possesses identical C-N bond lengths.
Applications
Several drug or drug candidates feature amidine substituents. Examples include the antiprotozoal imidocarb, the insecticide amitraz, xylamidine, an antagonist at the 5HT2A receptor, and the anthelmintics amidantel and tribendimidine.Formamidinium may be reacted with a metal halide to form the light-absorbing semiconducting material in perovskite [solar cell]s. Formamidinium cations or halides may partially or fully replace methylammonium halides in forming perovskite absorber layers in photovoltaic devices.